Clinical Research Specialist
2 days ago
Title: Clinical Research Specialist
Location: 100% REMOTE ROLE
Contract: 24 months of contract to start with possible extension
Job Summary:
• Individual will be supporting the Neurovascular Operating Unit here at client and will be responsible for site management duties.
• Individual will serve as main contact for sites assigned to their care and ensuring sites are prepared for study participants, answer site questions, ensure site milestones are met.
Hiring Manager Top 3 skills:
1. Site Management experience (site or sponsor)
2. Knowledge of/experience with CTMS/EDC/TMF
3. Experience with Good Clinical Practice (GCP)
Education Required:
• Bachelor Degree
Years of experience needed:
• Minimum 2 years with Bachelor’s degree and 0 years experience with advanced degree.
Responsibilities may include the following and other duties may be assigned:
• Oversees, designs, plans and develops clinical evaluation research studies.
• Prepares and authors protocols and patient record forms.
• Conducts registered and nonregistered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential.
• Oversees and interpret results of clinical investigations in preparation for new drug device or consumer application. Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets.
• May be responsible for clinical supply operations, site and vendor selection.
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